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Increased expression of p62/SQSTM1 in prion diseases and its association with pathogenic prion protein

Prion diseases are neurodegenerative disorders characterized by the aggregation of abnormally folded prion protein (PrP(Sc)). In this study, we focused on the mechanism of clearance of PrP(Sc), which remains unclear. p62 is a cytosolic protein known to mediate both the formation and degradation of a...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Homma, Takujiro, Ishibashi, Daisuke, Nakagaki, Takehiro, Satoh, Katsuya, Sano, Kazunori, Atarashi, Ryuichiro, Nishida, Noriyuki
التنسيق: Artigo
اللغة:Inglês
منشور في: Nature Publishing Group 2014
الموضوعات:
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC3968452/
https://ncbi.nlm.nih.gov/pubmed/24675871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep04504
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